Canonical Allele Identifier: CA1546666429

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658821C= , CM000667.2:g.53658821C=	GRCh38
NC_000005.9:g.52954651C= , CM000667.1:g.52954651C=	GRCh37
NC_000005.8:g.52990408C=	NCBI36
NG_008200.1:g.103187C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.424+197C= MANE Select	ENSP00000296684.5:n.424+197C=
ENST00000296684.9:c.424+197C=	ENSP00000296684.5:n.424+197C=
ENST00000502423.5:c.*291+197C=	ENSP00000422177.1:n.*291+197C=
ENST00000506765.1:c.338+12416C=	ENSP00000424570.1:n.338+12416C=
ENST00000506974.5:c.*200+197C=	ENSP00000425967.1:n.*200+197C=
ENST00000507026.5:c.*398+197C=	ENSP00000424993.1:n.*398+197C=
NM_002495.2:c.424+197C=	NP_002486.1:n.424+197C=
XM_005248525.3:c.350+12416C=	XP_005248582.1:n.350+12416C=
XM_011543415.1:c.250+197C=	XP_011541717.1:n.250+197C=
NM_001318051.1:c.350+12416C=	NP_001304980.1:n.350+12416C=
NM_002495.3:c.424+197C=	NP_002486.1:n.424+197C=
NR_134473.1:n.626+197C=
NR_134474.1:n.543+197C=
NR_134475.1:n.578+197C=
NM_002495.4:c.424+197C= MANE Select	NP_002486.1:n.424+197C=
NM_001318051.2:c.350+12416C=	NP_001304980.1:n.350+12416C=
NR_134473.2:n.620+197C=
NR_134474.2:n.537+197C=
NR_134475.2:n.572+197C=